Evidence map›Paper›PMID 11602471›Full record

ArticleAnnals of the rheumatic diseases2001

Impaired redox status and cytochrome c oxidase deficiency in patients with polymyalgia rheumatica.

P Chariot, X Chevalier, M Yerroum, I Drogou, F J Authier, R Gherardi

Open access · bronzeAbstract read
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Article in Annals of the rheumatic diseases, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

P ChariotDepartment of Pathology (Neuromuscular Disorders), Hôpital Henri-Mondor, 94000 Créteil, France. pchariot@cybercable.fr
X Chevalier
M Yerroum
I Drogou
F J Authier
R Gherardi
Hôpitaux Universitaires Henri-Mondor · FRAssistance Publique – Hôpitaux de Paris · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate redox status and muscular mitochondrial abnormalities in patients with polymyalgia rheumatica (PMR).

methodsProspective evaluation of deltoid muscle biopsy in 15 patients with PMR. Fifteen subjects matched for age and sex, with histologically normal muscle and without clinical evidence of myopathy, were used as controls. Cryostat sections of muscle were processed for conventional dyes, cytochrome c oxidase (COX), usual histochemical reactions, and Sudan black. A total of 300-800 fibres was examined in each case. Blood lactate, pyruvate, and lactate/pyruvate ratio were determined in all patients.

resultsRagged red fibres were found in eight patients with PMR and accounted for 0-0.5% of fibres. Focal COX deficiency was found in 14 (93%) of 15 patients and in nine (60%) of 15 controls. COX deficient fibres were more common in patients with PMR (range 0-2.5%; mean 0.9%) than in controls (range 0-1.2%; mean 0.3%) (paired t test, p=0.001). Seven (47%) of 15 patients had high blood lactate levels (1.50-2.60 mmol/l) or high blood lactate/pyruvate ratios (22-25).

conclusionsPMR is associated with mitochondrial abnormalities not solely related to the aging process.

Indexed as

Cytochrome-c Oxidase DeficiencyAgedAged, 80 and overBiopsyCase-Control StudiesFemaleHumansLactic AcidMaleMiddle AgedMuscle Fibers, Fast-TwitchMuscle, SkeletalOxidation-ReductionPolymyalgia RheumaticaProspective StudiesPyruvic AcidLactic AcidPyruvic AcidSuccinate Dehydrogenase

Identifiers

PMID11602471
PMCPMC1753428
OpenAlexW1985655250

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.